NDC 16590-856 Pentoxifylline
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Product Details
What is NDC 16590-856?
What are the uses for Pentoxifylline?
Which are Pentoxifylline UNII Codes?
The UNII codes for the active ingredients in this product are:
- PENTOXIFYLLINE (UNII: SD6QCT3TSU)
- PENTOXIFYLLINE (UNII: SD6QCT3TSU) (Active Moiety)
Which are Pentoxifylline Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Pentoxifylline?
- RxCUI: 312301 - pentoxifylline 400 MG Extended Release Oral Tablet
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".